Diabetes technology

Determination of Glucose-Independent Racial Disparity in HbA1c for Youth With Type 1 Diabetes in the Era of Continuous Glucose Monitoring

J Diabetes Sci TechnolPublished Cross-sectional study

Authors' conclusion

Young B patients have clinically relevant higher average HbA1c at any given level of MBG or TIR than W patients, which may pose an additional risk for diabetes complications development. HGI ≥ 0.5 may be an easy way to identify high-risk patients.

Study context

Population
Healthy youth with T1D using factory-calibrated continuous glucose monitoring (CGM); age 14.7 ± 4.8 years, M/F = 51/67, diabetes duration 5.4 ± 4.7 years
Participants
33 vs 85
Exposure
Non-Hispanic black vs non-Hispanic white youth with T1D
  • Bn = 33
  • Wn = 85reference
Outcome
HbA1c adjusted for MBG, age, gender, insulin delivery method and race by percent sensor use interaction

Main finding

As reported in the abstract

Average HbA1c adjusted for MBG, age, gender, insulin delivery method and race by PSU interaction

P < 0.0001

Observational data: associations, not effects.

Further findings

Unadjusted glycaemic measures

B had higher unadjusted HbA1c, mean blood glucose (MBG), MBGSD, glucose management index (GMI) and hemoglobin glycation index (HGI) than W
Time in range (TIR) and percent sensor use were lower for B
Time below range was similar for both

HbA1c with TIR substituted for MBG; predicted MBG

Higher HbA1c persisted in B when TIR was substituted for MBG
Predicted MBG higher in B at any level of percent sensor use (PSU)

Hemoglobin glycation index (HGI)

95th percentile of HGI in W
0.47
B with HGI ≥ 0.5
52%

Original publication

Determination of Glucose-Independent Racial Disparity in HbA1c for Youth With Type 1 Diabetes in the Era of Continuous Glucose Monitoring. J Diabetes Sci Technol. Published 12 September 2023. doi:10.1177/19322968231199113

Composed by AI from the published abstract and checked against it. How Briefs are made →

Get them every week

New studies on this topic in My Week and in your Monday e-mail.

We e-mail you a sign-in link and a code. No password, no spam.